Article L6311-3
The purpose of the access to care service is to assess the health needs of any person who requests it, to provide them with appropriate advice and to arrange for care appropriate to their condition.It…
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Showing 4001–4010 of 68091 articles for “Art. s. L 233-3 and R 225-31”
The purpose of the access to care service is to assess the health needs of any person who requests it, to provide them with appropriate advice and to arrange for care appropriate to their condition.It…
Without prejudice to the provisions relating to dismissal for disciplinary misconduct or professional inadequacy mentioned in articles R. 6152-370 and R. 6152-372, the dismissal of a practitioner with…
The occupational physician's role is exclusively preventive. It consists of preventing any deterioration in the health of workers as a result of their work, in particular by monitoring their hygiene c…
In accordance with the provisions ofarticle 34 of order no. 2016-65 of 29 January 2016 on concession contracts, the term of these contracts is adjusted according to the nature and scale of the investm…
Where a trader subject to the provisions of Chapter I of Title II of Book II is manifestly unable to comply with his obligations under Article L. 221-15, the administrative authority responsible for c…
The declaration provided for in Article L. 123-29 is sent by registered letter with acknowledgement of receipt or delivered against receipt.If the application is incomplete, the regional chamber of co…
After the marketing authorisation has been granted, the marketing authorisation holder must immediately forward to the National Agency for the Safety of Medicines and Health Products, indicating the s…
The Director General of the Agence nationale de sécurité du médicament et des produits de santé may require samples and mock-ups to be submitted when the medicinal product is marketed.
The marketing authorisation issued by the Agence nationale de sécurité du médicament et des produits de santé lapses if it transpires that: 1° That it is not followed by the marketing of the medicinal…
The marketing authorisation may impose one or more of the following conditions, which must be mentioned in the risk management system: 1° The implementation of measures to ensure the safe use of the m…
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